Canonical Allele Identifier: CA6058118
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs138508109
ExAC: 11:62622483 C / T
gnomAD v2: 11-62622483-C-T
gnomAD v4: 11-62855011-C-T
COSMIC: COSN160465
MyVariant Identifiers: chr11:g.62622483C>T (hg19) chr11:g.62855011C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855011C>T , CM000673.2:g.62855011C>T GRCh38
NC_000011.9:g.62622483C>T , CM000673.1:g.62622483C>T GRCh37
NC_000011.8:g.62379059C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.152-73G>A
NR_003098.2:n.149-73G>A
NR_152575.1:n.547-73G>A
NR_152576.1:n.539-73G>A
NR_152577.1:n.148+122G>A
NR_152578.1:n.105+122G>A
NR_152579.1:n.148+122G>A
NR_152580.1:n.148+122G>A
NR_152581.1:n.149-73G>A
NR_152582.1:n.106-73G>A
NR_152583.1:n.148+122G>A
NR_152584.1:n.547-73G>A
NR_152585.1:n.546+122G>A
Search 100 bp 5'
Search 100 bp 3'